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Publications

Targeting the 5′ untranslated region of SMN2 as a therapeutic strategy for spinal muscular atrophy

Winkelsas AM. et al, (2021), Molecular Therapy - Nucleic Acids, 23, 731 - 742

Regional lithium prescription rates and recurrence in bipolar disorder

Goodwin GM., (2021), International Journal of Bipolar Disorders

Disentangling the complex bidirectional associations between COVID-19 and psychiatric disorder - Authors' reply.

Taquet M. et al, (2021), Lancet Psychiatry, 8

Feasibility and efficacy of a digital CBT intervention for symptoms of Generalized Anxiety Disorder: A randomized multiple-baseline study.

Miller CB. et al, (2021), J Behav Ther Exp Psychiatry, 70

Nanoscale Amperometry Reveals that Only a Fraction of Vesicular Serotonin Content is Released During Exocytosis from Beta Cells

Hatamie A. et al, (2021), Angewandte Chemie

Participatory design to create a VR therapy for psychosis

Knight I. et al, (2021), Design for Health, 1 - 22

Excitatory neuronal CHD8 in the regulation of neocortical development and sensory-motor behaviors.

Kweon H. et al, (2021), Cell Rep, 34

Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers

Cosgrave J. et al, (2021), Journal of Sleep Research

Waking experience modulates sleep need in mice

BANNERMAN D. et al, (2021), BMC Biology

Psilocin acutely disrupts sleep and affects local but not global sleep homeostasis in laboratory mice

Thomas CW. et al, (2021)

Pregnancy-related interventions in mothers at risk for gestational diabetes in Asian India and low and middle-income countries (PRIMORDIAL study): protocol for a randomised controlled trial.

Vasan SK. et al, (2021), BMJ Open, 11

Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP study.

Kraus SM. et al, (2021), Int J Cardiol

Author Correction: Voltage-independent GluN2A-type NMDA receptor Ca2+ signaling promotes audiogenic seizures, attentional and cognitive deficits in mice.

Bertocchi I. et al, (2021), Commun Biol, 4, 187 - 187

Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophy.

Himič V. and Davies KE., (2021), Eur J Hum Genet

Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Lagou V. et al, (2021), Nat Commun, 12

Functional analysis of a gene-edited mouse to gain insights into the disease mechanisms of a titin missense variant

JIANG H. et al, (2021), Basic Research in Cardiology

Akr1d1-/-mice have a sexually dimorphic metabolic phenotype with reduced fat mass, increased insulin sensitivity and hypertriglyceridemia in males

Gathercole LL. et al, (2021), bioRxiv, 2021.02.02.429227 - 2021.02.02.429227

A fine balance between Prpf19 and Exoc7 in achieving degradation of aggregated protein and suppression of cell death in spinocerebellar ataxia type 3.

Chen ZS. et al, (2021), Cell Death Dis, 12

A new perspective and assessment measure for common dissociative experiences: ‘Felt Sense of Anomaly’

Cernis E. et al, (2021), PLoS One

Author Correction: Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals.

Whiffin N. et al, (2021), Nat Commun, 12

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